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“Hexacath” Merak LD PTA Dilatation Catheter - Taiwan Registration 5c529a537df77afa135a0472dadac3ef

Access comprehensive regulatory information for “Hexacath” Merak LD PTA Dilatation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5c529a537df77afa135a0472dadac3ef and manufactured by Hexacath. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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5c529a537df77afa135a0472dadac3ef
Registration Details
Taiwan FDA Registration: 5c529a537df77afa135a0472dadac3ef
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Device Details

“Hexacath” Merak LD PTA Dilatation Catheter
TW: “海斯凱” 翼星周邊血管球囊擴張導管
Risk Class 2
MD

Registration Details

5c529a537df77afa135a0472dadac3ef

Ministry of Health Medical Device Import No. 034852

DHA05603485203

Company Information

France

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Sep 07, 2021

Sep 07, 2026